Climate warming increases global oceanic dimethyl sulfide emissions

Oceanic dimethyl sulfide (DMS) is the largest natural source of atmospheric sulfur. DMS is biologically produced in seawater and emitted into the atmosphere, where its oxidation products contribute to aerosol formation with consequences for cloud albedo and the Earth's radiative budget and climate. Climate model projections of how DMS emissions change with global warming are largely uncertain, even contradictory. Here, we use machine-learning models trained with biome-resolved global observations to simulate seawater DMS concentrations (1850 to 2100) using physico-chemical and biological predictors from eight CMIP6 models. The scatter in current projections is largely reduced, and globally averaged seawater DMS concentrations are predicted to decrease in the coming decades. However, global DMS emissions will increase due to rising surface wind speeds and sea surface temperatures which contradicts the current AR6 assessment that the DMS flux will reduce in the future. Concurrence of increasing DMS emissions and declining anthropogenic sulfur dioxide emissions suggests an increase in the relative importance of DMS to sulfate aerosol formation and its climate cooling impact.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-06-02
DOI
https://doi.org/10.1073/pnas.2502077122
Citations
4
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
5.20
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article

Climate warming increases global oceanic dimethyl sulfide emissions

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4 citations
Proceedings of the National Academy of Sciences
Atmospheric chemistry and aerosols
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article

Climate warming increases global oceanic dimethyl sulfide emissions

Sankirna D. Joge, Alfonso Saiz‐Lopez, Rafel Simó, Nadja Steiner, Karam Mansour, Anoop S. Mahajan, Martí Galí
article en
4 citations

Abstract

Oceanic dimethyl sulfide (DMS) is the largest natural source of atmospheric sulfur. DMS is biologically produced in seawater and emitted into the atmosphere, where its oxidation products contribute to aerosol formation with consequences for cloud albedo and the Earth's radiative budget and climate. Climate model projections of how DMS emissions change with global warming are largely uncertain, even contradictory. Here, we use machine-learning models trained with biome-resolved global observations to simulate seawater DMS concentrations (1850 to 2100) using physico-chemical and biological predictors from eight CMIP6 models. The scatter in current projections is largely reduced, and globally averaged seawater DMS concentrations are predicted to decrease in the coming decades. However, global DMS emissions will increase due to rising surface wind speeds and sea surface temperatures which contradicts the current AR6 assessment that the DMS flux will reduce in the future. Concurrence of increasing DMS emissions and declining anthropogenic sulfur dioxide emissions suggests an increase in the relative importance of DMS to sulfate aerosol formation and its climate cooling impact.

Proceedings of the National Academy of SciencesVol. 122(23)
Fisheries and Oceans Canada (CA), Indian Institute of Tropical Meteorology (IN), Consejo Superior de Investigaciones Científicas (ES), National Academies of Sciences, Engineering, and Medicine (US), Institute of Atmospheric Sciences and Climate (IT), Ministry of Earth Sciences (IN), Institut de Ciències del Mar (ES), Alexandria University (EG), Savitribai Phule Pune University (IN)
Life below water
Openalex Percentile: Top 4%
Atmospheric chemistry and aerosols
5.20
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